Analyst, QC

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation. Learn new skills and capabilities. Grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video. What you’ll get An agile career and dynamic working culture in a global life sciences leader. An inclusive and ethical workplace that values diversity and integrity. Competitive compensation programs that recognize high performance. Professional growth opportunities through cross-functional projects and global exposure. Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums. Company transport provided from designated MRT locations to and from the Tuas site. Access to Lonza’s full suite of employee benefits: What you’ll do Prioritize and execute various testing and analyses in a timely manner to meet business requirements. Conduct analysis of final products, in-process materials, raw materials, and environmental samples in accordance with Standard Operating Procedures (SOPs) and Test Methods. Document and review results in compliance with current Good Manufacturing Practices (cGMP). Provide general laboratory support, including housekeeping, equipment maintenance, inventory management, ordering lab supplies, managing glassware, and autoclaving. Support sample logistics, including retention sample storage, coordination of external lab tests, QC document control, and QC sample shipments. Prepare and maintain standards and reagents as per GMP documentation. Ensure compliance with data integrity requirements. Actively contribute to operational efficiency and continuous improvement initiatives. Perform additional duties as assigned by the Manager. Troubleshoot analytical methods and laboratory equipment issues. Participate in equipment qualification, maintenance, and troubleshooting. Conduct and support Out-of-Specification (OOS) and deviation investigations, including drafting investigation reports. Participate in method transfers and validation processes. What we’re looking for Degree in Chemistry or Biological Chemistry. Relevant work experience preferably with Raw Material handling Understanding and execution of compendial monographs and the chemistry fundamentals behind methods. Technology/equipment, UV, Infrared Spectroscopy, Osmolality, HPLC, pH, Conductivity, Polarimetry, Refractometry, Density meter, Titration (manual and automatic), as well as all compendial testing listed in the USP, JP and EP monographs. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. #J-18808-Ljbffr